Your browser doesn't support javascript.
loading
[Genetic analysis of microcephaly-cortical blind syndrome due to compound heterozygous variants of DIAPH1 gene].
Li, Xiaobing; Lai, Panjian; Cheng, Kaichao; Wang, Dayan.
Affiliation
  • Li X; Third Ward of Pediatric Medicine, Jinhua Maternal and Child Health Care Hospital, Jinhua, Zhejiang 321000, China. airy005@163.com.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 39(10): 1116-1119, 2022 Oct 10.
Article in Zh | MEDLINE | ID: mdl-36184095
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Microcephaly Type of study: Prognostic_studies Limits: Child / Female / Humans Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: China Country of publication: China
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Microcephaly Type of study: Prognostic_studies Limits: Child / Female / Humans Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: China Country of publication: China